Egenskap
Lethargy
A state of fatigue, either physical or mental slowness and sluggishness, with difficulties in initiating or performing simple tasks. Distinguished from apathy which implies indifference and a lack of desire or interest in the task. A person with lethargy may have the desire, but not the energy to engage in personal or socially relevant tasks.
Sammendrag
- Også kalt
- Dullness, Inaction, Inactivity, Languor, Slowness, Torpor
- Kroppssystem
- Abnormality of the nervous system
ReferansegenomGRCh38hg38
Posisjoner på gen- og variantsidene følger dette valget i denne nettleseren.
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Få mitt Genome Test262 gener knyttet til Lethargy
Endringer i disse genene forårsaker sjeldne tilstander der Lethargy forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ABAT4-aminobutyrate aminotransferase | Alltid | I 2 tilstander |
| ACADVLacyl-CoA dehydrogenase very long chain | Alltid | I 2 tilstander |
| AK2adenylate kinase 2 | Alltid | I 1 tilstand |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Alltid | I 1 tilstand |
| ATP5F1DATP synthase F1 subunit delta | Alltid | I 2 tilstander |
| BCKDHBbranched chain keto acid dehydrogenase E1 subunit beta | Alltid | I 1 tilstand |
| BOLA3bolA family member 3 | Alltid | I 2 tilstander |
| COG8component of oligomeric golgi complex 8 | Alltid | I 1 tilstand |
| CPS1carbamoyl-phosphate synthase 1 | Alltid | I 1 tilstand |
| CPT1Acarnitine palmitoyltransferase 1A | Alltid | I 2 tilstander |
| DBTdihydrolipoamide branched chain transacylase E2 | Alltid | I 1 tilstand |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Alltid | I 1 tilstand |
| FDXRferredoxin reductase | Alltid | I 1 tilstand |
| GCSHglycine cleavage system protein H | Alltid | I 1 tilstand |
| HIBCH3-hydroxyisobutyryl-CoA hydrolase | Alltid | I 1 tilstand |
| LDB3LIM domain binding 3 | Alltid | I 1 tilstand |
| MRPS16mitochondrial ribosomal protein S16 | Alltid | I 1 tilstand |
| MTR5-methyltetrahydrofolate-homocysteine methyltransferase | Alltid | I 1 tilstand |
| NAGSN-acetylglutamate synthase | Alltid | I 2 tilstander |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Alltid | I 2 tilstander |
| NFS1NFS1 cysteine desulfurase | Alltid | I 1 tilstand |
| NFU1NFU1 iron-sulfur cluster scaffold | Alltid | I 1 tilstand |
| PDHA1pyruvate dehydrogenase E1 subunit alpha 1 | Alltid | I 1 tilstand |
| RAB32RAB32, member RAS oncogene family | Alltid | I 1 tilstand |
| SLC25A20solute carrier family 25 member 20 | Alltid | I 2 tilstander |
| SLC31A1solute carrier family 31 member 1 | Alltid | I 1 tilstand |
| SLC52A1solute carrier family 52 member 1 | Alltid | I 1 tilstand |
| TAMM41TAM41 mitochondrial translocator assembly and maintenance homolog | Alltid | I 1 tilstand |
| WSB2WD repeat and SOCS box containing 2 | Alltid | I 1 tilstand |
| FOXRED1FAD dependent oxidoreductase domain containing 1 | Svært ofte (80–99 %) | I 1 tilstand |
| HADHhydroxyacyl-CoA dehydrogenase | Svært ofte (80–99 %) | I 1 tilstand |
| HNF4Ahepatocyte nuclear factor 4 alpha | Svært ofte (80–99 %) | I 1 tilstand |
| MMADHCmetabolism of cobalamin associated D | Svært ofte (80–99 %) | I 2 tilstander |
| MMUTmethylmalonyl-CoA mutase | Svært ofte (80–99 %) | I 3 tilstander |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Svært ofte (80–99 %) | I 1 tilstand |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Svært ofte (80–99 %) | I 1 tilstand |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFA1NADH:ubiquinone oxidoreductase subunit A1 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFA11NADH:ubiquinone oxidoreductase subunit A11 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFA6NADH:ubiquinone oxidoreductase subunit A6 | Svært ofte (80–99 %) | I 1 tilstand |
Vis 222 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| NDUFA9NADH:ubiquinone oxidoreductase subunit A9 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF1NADH:ubiquinone oxidoreductase complex assembly factor 1 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF2NADH:ubiquinone oxidoreductase complex assembly factor 2 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF3NADH:ubiquinone oxidoreductase complex assembly factor 3 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF4NADH:ubiquinone oxidoreductase complex assembly factor 4 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF5NADH:ubiquinone oxidoreductase complex assembly factor 5 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF8NADH:ubiquinone oxidoreductase complex assembly factor 8 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFB10NADH:ubiquinone oxidoreductase subunit B10 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFB3NADH:ubiquinone oxidoreductase subunit B3 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFB9NADH:ubiquinone oxidoreductase subunit B9 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFS1NADH:ubiquinone oxidoreductase core subunit S1 | Svært ofte (80–99 %) | I 2 tilstander |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Svært ofte (80–99 %) | I 2 tilstander |
| NDUFS3NADH:ubiquinone oxidoreductase core subunit S3 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFS6NADH:ubiquinone oxidoreductase subunit S6 | Svært ofte (80–99 %) | I 2 tilstander |
| NDUFS7NADH:ubiquinone oxidoreductase core subunit S7 | Svært ofte (80–99 %) | I 2 tilstander |
| NDUFS8NADH:ubiquinone oxidoreductase core subunit S8 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFV1NADH:ubiquinone oxidoreductase core subunit V1 | Svært ofte (80–99 %) | I 2 tilstander |
| NDUFV2NADH:ubiquinone oxidoreductase core subunit V2 | Svært ofte (80–99 %) | I 1 tilstand |
| NUBPLNUBP iron-sulfur cluster assembly factor, mitochondrial | Svært ofte (80–99 %) | I 1 tilstand |
| SLC19A2solute carrier family 19 member 2 | Svært ofte (80–99 %) | I 1 tilstand |
| TIMMDC1translocase of inner mitochondrial membrane domain containing 1 | Svært ofte (80–99 %) | I 1 tilstand |
| TMEM126Btransmembrane protein 126B | Svært ofte (80–99 %) | I 1 tilstand |
| ABCD4ATP binding cassette subfamily D member 4 | Ofte (30–79 %) | I 1 tilstand |
| ACADSacyl-CoA dehydrogenase short chain | Ofte (30–79 %) | I 2 tilstander |
| ADA2adenosine deaminase 2 | Ofte (30–79 %) | I 1 tilstand |
| ARXaristaless related homeobox | Ofte (30–79 %) | I 1 tilstand |
| ASLargininosuccinate lyase | Ofte (30–79 %) | I 2 tilstander |
| ASPAaspartoacylase | Ofte (30–79 %) | I 1 tilstand |
| ATP13A2ATPase cation transporting 13A2 | Ofte (30–79 %) | I 1 tilstand |
| ATP5MKATP synthase membrane subunit k | Ofte (30–79 %) | I 2 tilstander |
| AVParginine vasopressin | Ofte (30–79 %) | I 1 tilstand |
| CA5Acarbonic anhydrase 5A | Ofte (30–79 %) | I 1 tilstand |
| CACNA1Ecalcium voltage-gated channel subunit alpha1 E | Ofte (30–79 %) | I 1 tilstand |
| CASKcalcium/calmodulin dependent serine protein kinase | Ofte (30–79 %) | I 1 tilstand |
| CDKL5cyclin dependent kinase like 5 | Ofte (30–79 %) | I 1 tilstand |
| CDONcell adhesion associated, oncogene regulated | Ofte (30–79 %) | I 4 tilstander |
| COX5Acytochrome c oxidase subunit 5A | Ofte (30–79 %) | I 1 tilstand |
| CPT2carnitine palmitoyltransferase 2 | Ofte (30–79 %) | I 2 tilstander |
| CRIPTOcripto, EGF-CFC family member | Ofte (30–79 %) | I 4 tilstander |
| DDCdopa decarboxylase | Ofte (30–79 %) | I 1 tilstand |
| DISP1dispatched RND transporter family member 1 | Ofte (30–79 %) | I 4 tilstander |
| DLDdihydrolipoamide dehydrogenase | Ofte (30–79 %) | I 2 tilstander |
| DLL1delta like canonical Notch ligand 1 | Ofte (30–79 %) | I 4 tilstander |
| DMXL2Dmx like 2 | Ofte (30–79 %) | I 1 tilstand |
| FGF8fibroblast growth factor 8 | Ofte (30–79 %) | I 4 tilstander |
| FGFR1fibroblast growth factor receptor 1 | Ofte (30–79 %) | I 2 tilstander |
| FHfumarate hydratase | Ofte (30–79 %) | I 1 tilstand |
| FOXE1forkhead box E1 | Ofte (30–79 %) | I 1 tilstand |
| FOXH1forkhead box H1 | Ofte (30–79 %) | I 4 tilstander |
| GAS1growth arrest specific 1 | Ofte (30–79 %) | I 4 tilstander |
| GATA1GATA binding protein 1 | Ofte (30–79 %) | I 1 tilstand |
| GLI2GLI family zinc finger 2 | Ofte (30–79 %) | I 4 tilstander |
| GNAO1G protein subunit alpha o1 | Ofte (30–79 %) | I 1 tilstand |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| GRM7glutamate metabotropic receptor 7 | Ofte (30–79 %) | I 1 tilstand |
| GUF1GTP binding elongation factor GUF1 | Ofte (30–79 %) | I 1 tilstand |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Ofte (30–79 %) | I 2 tilstander |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Ofte (30–79 %) | I 1 tilstand |
| HAMPhepcidin antimicrobial peptide | Ofte (30–79 %) | I 1 tilstand |
| HEATR3HEAT repeat containing 3 | Ofte (30–79 %) | I 1 tilstand |
| HESX1HESX homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| HJVhemojuvelin BMP co-receptor | Ofte (30–79 %) | I 2 tilstander |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Ofte (30–79 %) | I 1 tilstand |
| IVDisovaleryl-CoA dehydrogenase | Ofte (30–79 %) | I 2 tilstander |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Ofte (30–79 %) | I 1 tilstand |
| LGI1leucine rich glioma inactivated 1 | Ofte (30–79 %) | I 1 tilstand |
| LHX3LIM homeobox 3 | Ofte (30–79 %) | I 1 tilstand |
| LHX4LIM homeobox 4 | Ofte (30–79 %) | I 1 tilstand |
| LMBRD1LMBR1 domain containing 1 | Ofte (30–79 %) | I 2 tilstander |
| NAXDNAD(P)HX dehydratase | Ofte (30–79 %) | I 2 tilstander |
| NDE1nudE neurodevelopment protein 1 | Ofte (30–79 %) | I 1 tilstand |
| NEUROD2neuronal differentiation 2 | Ofte (30–79 %) | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| NKX2-5NK2 homeobox 5 | Ofte (30–79 %) | I 1 tilstand |
| NODALnodal growth differentiation factor | Ofte (30–79 %) | I 4 tilstander |
| OTCornithine transcarbamylase | Ofte (30–79 %) | I 2 tilstander |
| PAX8paired box 8 | Ofte (30–79 %) | I 2 tilstander |
| PIGPphosphatidylinositol glycan anchor biosynthesis class P | Ofte (30–79 %) | I 1 tilstand |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Ofte (30–79 %) | I 1 tilstand |
| PLCH1phospholipase C eta 1 | Ofte (30–79 %) | I 1 tilstand |
| PNKPpolynucleotide kinase 3'-phosphatase | Ofte (30–79 %) | I 1 tilstand |
| POU1F1POU class 1 homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| PROP1PROP paired-like homeobox 1 | Ofte (30–79 %) | I 1 tilstand |
| PTCH1patched 1 | Ofte (30–79 %) | I 4 tilstander |
| RARS2arginyl-tRNA synthetase 2, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| RHOBTB2Rho related BTB domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| RMND1required for meiotic nuclear division 1 homolog | Ofte (30–79 %) | I 1 tilstand |
| RPL11ribosomal protein L11 | Ofte (30–79 %) | I 1 tilstand |
| RPL15ribosomal protein L15 | Ofte (30–79 %) | I 1 tilstand |
| RPL18ribosomal protein L18 | Ofte (30–79 %) | I 1 tilstand |
| RPL26ribosomal protein L26 | Ofte (30–79 %) | I 1 tilstand |
| RPL27ribosomal protein L27 | Ofte (30–79 %) | I 1 tilstand |
| RPL31ribosomal protein L31 | Ofte (30–79 %) | I 1 tilstand |
| RPL35ribosomal protein L35 | Ofte (30–79 %) | I 1 tilstand |
| RPL35Aribosomal protein L35a | Ofte (30–79 %) | I 1 tilstand |
| RPL5ribosomal protein L5 | Ofte (30–79 %) | I 1 tilstand |
| RPL8ribosomal protein L8 | Ofte (30–79 %) | I 1 tilstand |
| RPL9ribosomal protein L9 | Ofte (30–79 %) | I 1 tilstand |
| RPS10ribosomal protein S10 | Ofte (30–79 %) | I 1 tilstand |
| RPS15Aribosomal protein S15a | Ofte (30–79 %) | I 1 tilstand |
| RPS17ribosomal protein S17 | Ofte (30–79 %) | I 1 tilstand |
| RPS19ribosomal protein S19 | Ofte (30–79 %) | I 1 tilstand |
| RPS20ribosomal protein S20 | Ofte (30–79 %) | I 1 tilstand |
| RPS24ribosomal protein S24 | Ofte (30–79 %) | I 1 tilstand |
| RPS26ribosomal protein S26 | Ofte (30–79 %) | I 1 tilstand |
| RPS27ribosomal protein S27 | Ofte (30–79 %) | I 1 tilstand |
| RPS28ribosomal protein S28 | Ofte (30–79 %) | I 1 tilstand |
| RPS29ribosomal protein S29 | Ofte (30–79 %) | I 1 tilstand |
| RPS7ribosomal protein S7 | Ofte (30–79 %) | I 1 tilstand |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Ofte (30–79 %) | I 1 tilstand |
| SHHsonic hedgehog signaling molecule | Ofte (30–79 %) | I 4 tilstander |
| SIK1salt inducible kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| SIX3SIX homeobox 3 | Ofte (30–79 %) | I 4 tilstander |
| SLC19A3solute carrier family 19 member 3 | Ofte (30–79 %) | I 1 tilstand |
| SLC25A13solute carrier family 25 member 13 | Ofte (30–79 %) | I 1 tilstand |
| SLC25A15solute carrier family 25 member 15 | Ofte (30–79 %) | I 2 tilstander |
| SLC25A22solute carrier family 25 member 22 | Ofte (30–79 %) | I 1 tilstand |
| SLC26A4solute carrier family 26 member 4 | Ofte (30–79 %) | I 1 tilstand |
| SLC2A1solute carrier family 2 member 1 | Ofte (30–79 %) | I 2 tilstander |
| SLC32A1solute carrier family 32 member 1 | Ofte (30–79 %) | I 1 tilstand |
| SMC1Astructural maintenance of chromosomes 1A | Ofte (30–79 %) | I 1 tilstand |
| STAG2STAG2 cohesin complex component | Ofte (30–79 %) | I 2 tilstander |
| STILSTIL centriolar assembly protein | Ofte (30–79 %) | I 4 tilstander |
| TFAMtranscription factor A, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| TGIF1TGFB induced factor homeobox 1 | Ofte (30–79 %) | I 4 tilstander |
| THtyrosine hydroxylase | Ofte (30–79 %) | I 1 tilstand |
| TRHRthyrotropin releasing hormone receptor | Ofte (30–79 %) | I 2 tilstander |
| TRIM8tripartite motif containing 8 | Ofte (30–79 %) | I 1 tilstand |
| TSHRthyroid stimulating hormone receptor | Ofte (30–79 %) | I 2 tilstander |
| TSPOAP1TSPO associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| TSR2TSR2 ribosome maturation factor | Ofte (30–79 %) | I 1 tilstand |
| YARS2tyrosyl-tRNA synthetase 2 | Ofte (30–79 %) | I 1 tilstand |
| ZIC2Zic family zinc finger 2 | Ofte (30–79 %) | I 4 tilstander |
| ABCC8ATP binding cassette subfamily C member 8 | Noen ganger (5–29 %) | I 1 tilstand |
| ACADMacyl-CoA dehydrogenase medium chain | Noen ganger (5–29 %) | I 2 tilstander |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Noen ganger (5–29 %) | I 1 tilstand |
| ATP5F1AATP synthase F1 subunit alpha | Noen ganger (5–29 %) | I 1 tilstand |
| ATP5F1EATP synthase F1 subunit epsilon | Noen ganger (5–29 %) | I 1 tilstand |
| ATP5POATP synthase peripheral stalk subunit OSCP | Noen ganger (5–29 %) | I 1 tilstand |
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| BMP6bone morphogenetic protein 6 | Noen ganger (5–29 %) | I 1 tilstand |
| BTDbiotinidase | Noen ganger (5–29 %) | I 2 tilstander |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Noen ganger (5–29 %) | I 1 tilstand |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Noen ganger (5–29 %) | I 1 tilstand |
| DUOX2dual oxidase 2 | Noen ganger (5–29 %) | I 2 tilstander |
| DUOXA2dual oxidase maturation factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GALTgalactose-1-phosphate uridylyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| GYS2glycogen synthase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| HFEhomeostatic iron regulator | Noen ganger (5–29 %) | I 1 tilstand |
| HLCSholocarboxylase synthetase | Noen ganger (5–29 %) | I 2 tilstander |
| HNF1AHNF1 homeobox A | Noen ganger (5–29 %) | I 1 tilstand |
| IYDiodotyrosine deiodinase | Noen ganger (5–29 %) | I 1 tilstand |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Noen ganger (5–29 %) | I 1 tilstand |
| MAGEL2MAGE family member L2 | Noen ganger (5–29 %) | I 1 tilstand |
| MEN1menin 1 | Noen ganger (5–29 %) | I 2 tilstander |
| MLYCDmalonyl-CoA decarboxylase | Noen ganger (5–29 %) | I 1 tilstand |
| MMACHCmetabolism of cobalamin associated C | Noen ganger (5–29 %) | I 2 tilstander |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | Noen ganger (5–29 %) | I 1 tilstand |
| MTHFRmethylenetetrahydrofolate reductase | Noen ganger (5–29 %) | I 1 tilstand |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Noen ganger (5–29 %) | I 2 tilstander |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| OXCT13-oxoacid CoA-transferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PAX2paired box 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PBX1PBX homeobox 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PCK1phosphoenolpyruvate carboxykinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PCK2phosphoenolpyruvate carboxykinase 2, mitochondrial | Noen ganger (5–29 %) | I 1 tilstand |
| PEX2peroxisomal biogenesis factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Noen ganger (5–29 %) | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| POLG2DNA polymerase gamma 2, accessory subunit | Noen ganger (5–29 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Noen ganger (5–29 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Noen ganger (5–29 %) | I 2 tilstander |
| SIM1SIM bHLH transcription factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC25A4solute carrier family 25 member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC5A5solute carrier family 5 member 5 | Noen ganger (5–29 %) | I 2 tilstander |
| SLC7A7solute carrier family 7 member 7 | Noen ganger (5–29 %) | I 1 tilstand |
| SUGCTsuccinyl-CoA:glutarate-CoA transferase | Noen ganger (5–29 %) | I 1 tilstand |
| TGthyroglobulin | Noen ganger (5–29 %) | I 1 tilstand |
| TPOthyroid peroxidase | Noen ganger (5–29 %) | I 1 tilstand |
| TSHBthyroid stimulating hormone subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Noen ganger (5–29 %) | I 1 tilstand |
| UCP2uncoupling protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| YY1YY1 transcription factor | Noen ganger (5–29 %) | I 1 tilstand |
| ALDOBaldolase, fructose-bisphosphate B | Sjelden (1–4%) | I 2 tilstander |
| BNC2basonuclin zinc finger protein 2 | Sjelden (1–4%) | I 1 tilstand |
| DPYDdihydropyrimidine dehydrogenase | Sjelden (1–4%) | I 1 tilstand |
| MT-CYBmitochondrially encoded cytochrome b | Sjelden (1–4%) | I 1 tilstand |
| ACADSBacyl-CoA dehydrogenase short/branched chain | Ikke registrert | I 1 tilstand |
| ASS1argininosuccinate synthase 1 | Ikke registrert | I 1 tilstand |
| BCKDHAbranched chain keto acid dehydrogenase E1 subunit alpha | Ikke registrert | I 1 tilstand |
| CYP24A1cytochrome P450 family 24 subfamily A member 1 | Ikke registrert | I 1 tilstand |
| DPYSdihydropyrimidinase | Ikke registrert | I 1 tilstand |
| EIF2B1eukaryotic translation initiation factor 2B subunit alpha | Ikke registrert | I 1 tilstand |
| FBP1fructose-bisphosphatase 1 | Ikke registrert | I 1 tilstand |
| GABRB2gamma-aminobutyric acid type A receptor subunit beta2 | Ikke registrert | I 1 tilstand |
| GCH1GTP cyclohydrolase 1 | Ikke registrert | I 1 tilstand |
| GKglycerol kinase | Ikke registrert | I 1 tilstand |
| GLDCglycine decarboxylase | Ikke registrert | I 1 tilstand |
| KRT18keratin 18 | Ikke registrert | I 1 tilstand |
| LYRM7LYR motif containing 7 | Ikke registrert | I 1 tilstand |
| MCCC1methylcrotonyl-CoA carboxylase subunit 1 | Ikke registrert | I 1 tilstand |
| MCCC2methylcrotonyl-CoA carboxylase subunit 2 | Ikke registrert | I 1 tilstand |
| MMAAmetabolism of cobalamin associated A | Ikke registrert | I 1 tilstand |
| MMABmetabolism of cobalamin associated B | Ikke registrert | I 1 tilstand |
| NBASNBAS subunit of NRZ tethering complex | Ikke registrert | I 1 tilstand |
| PCCApropionyl-CoA carboxylase subunit alpha | Ikke registrert | I 1 tilstand |
| PCCBpropionyl-CoA carboxylase subunit beta | Ikke registrert | I 1 tilstand |
| PRDX1peroxiredoxin 1 | Ikke registrert | I 1 tilstand |
| SLC1A2solute carrier family 1 member 2 | Ikke registrert | I 1 tilstand |
| SLC22A5solute carrier family 22 member 5 | Ikke registrert | I 1 tilstand |
| SLC25A19solute carrier family 25 member 19 | Ikke registrert | I 1 tilstand |
| SLC39A4solute carrier family 39 member 4 | Ikke registrert | I 1 tilstand |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Ikke registrert | I 1 tilstand |
| TBK1TANK binding kinase 1 | Ikke registrert | I 1 tilstand |
| TCN2transcobalamin 2 | Ikke registrert | I 1 tilstand |
| TLR3toll like receptor 3 | Ikke registrert | I 1 tilstand |
| USP18ubiquitin specific peptidase 18 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
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- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.16-c6eea6bf.
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